Quality Assurance Specialist

JR United Kingdom; West Midlands Combined Authority; On-site; GBP 30,000 - 45,000; Full time

Job summary

A leading company in the pharmaceutical industry is looking for a Quality Assurance Specialist to join their Global Development Quality team. This role involves ensuring compliance with GMP standards and contributing to the delivery of vital treatments. The ideal candidate will have a scientific background, exceptional attention to detail, and strong communication skills. If you are motivated and ready to make an impact in the field of quality assurance, apply now.

Qualifications

• Bachelor’s degree in Chemistry, Biology, Pharmacy or related field.
• Strong attention to detail and communication skills.
• Experience working independently.

Responsibilities

• Perform final review of clinical batch records for compliance.
• Compile and approve data packs for QP release.
• Collaborate with clinical supply chain teams.

Skills

Attention to detail

Organizational skills

Communication

Interpersonal abilities

Ability to manage multiple priorities

Education

Bachelor’s degree in a scientific discipline

Job description

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Quality Assurance Specialist, west midlands

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Client:

Planet Pharma

Location:

Job Category:

Other

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EU work permit required:

Yes

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Job Views:

1

Posted:

04.06.2025

Expiry Date:

19.07.2025

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Job Description:

An exciting opportunity is available for a motivated and detail-oriented Quality Specialist to join a Global Development Quality team. This role offers exposure to a wide range of investigational medicinal products, from small molecules to advanced immunotherapies, contributing directly to the delivery of life-saving treatments to patients.

Key Responsibilities:

• Perform final review of clinical batch records to ensure compliance with GMP and regulatory filings.
• Compile and approve data packs for Qualified Person (QP) release.
• Collaborate with global clinical supply chain teams and manufacturing sites (internal and external).
• Manage issue resolution and ensure timely documentation and communication.
• Maintain high standards of accuracy and compliance throughout the review process.

Qualifications & Skills:

Required:

• Bachelor’s degree in a scientific discipline (e.g., Chemistry, Biology, Pharmacy).
• Strong attention to detail and organizational skills.
• Excellent communication and interpersonal abilities.
• Ability to work independently and manage multiple priorities.

Preferred:

• Prior experience in a QA or GMP-regulated environment.
• Familiarity with clinical manufacturing and regulatory compliance processes.